Variant #0010906977 (NC_000017.10:g.79108258G>C, NM_001080395.2:c.99C>G (AATK))

Chromosome 17
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.79108258G>C
DB-ID -
dbSNP ID rs763434510
gnomAD frequency 1/244498
gnomAD homozygote count 0/122246
Average frequency (gnomAD v.2.1.1) Retrieve
Database submission license No license selected
Created by LOVD
Date created 2017-02-27 00:00:00 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
AATK NM_001080395.2 ./. c.99C>G r.(?) p.(Ala33=)
AATK NM_004920.2 ./. c.-2677C>G r.(=) p.(=)